Decree of the Government of the Czech Socialist Republic No. 192 / 1988 Coll.
Decree of the Government of the Czech Socialist Republic on poisons and certain other harmful health substances
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Effective from 01.01.1989
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192
GOVERNMENT REGULATION
Czech Socialist Republic
of 19 October 1988
on poisons and certain other harmful health substances
The Government of the Czech Socialist Republic orders according to § 4 paragraphs 3 and 4 and § 82 of Act No. 20 / 1966 Coll., on the care of the health of the people:
BASIC PROVISIONS
(1) This Regulation provides for the treatment of poisons and certain other harmful substances and provides for protective measures. Some other harmful substances are corrosive substances, narcotic substances and psychotropic substances.
(2) Under this Regulation:
(a) poisons of substances that cause poisoning already in small doses; are divided into particularly dangerous poisons and other poisons and are included in the lists of these substances;
(b) corrosive substances such as those which severely harm tissues which come into direct contact;
(c) narcotic substances and psychotropic substances of those substances which present a risk of disease or psychological changes which are dangerous to society or to those who repeatedly use them without professional supervision and are listed in those substances.
(3) The lists of particularly dangerous poisons, other poisons, narcotic drugs and psychotropic substances are set out in Annexes 1 to 4 to this Regulation.
(4) The preparation shall mean for the purposes of this Regulation a solution or mixture containing one or more of the substances referred to in paragraph 2 and having its properties.
(5) The treatment of the substances referred to in paragraph 2 and preparations for the purposes of this Regulation means their production, research, development, transport, processing, supply, sale, storage, import and any other use.
(6) The provisions of Part Two of this Regulation are not applicable to the medicinal product, 1) if it is also a poison, corrosive, narcotic or psychotropic substance or preparation.
(7) Explosive, (2) if it is also poison, corrosive or preparation, shall not be subject to the provisions of this Regulation except for Part One.
(1) In the treatment of substances referred to in § 1 (2) and preparations, everyone shall be obliged to proceed in such a way as not to harm the health of humans, in particular the health, in particular the biological value of the food and objects of normal use, the health of the air, the water (3) and the soil, so as not to endanger livestock, wild animals, (4) animals and protected species of plants, (5) to prevent the misuse of such substances or preparations.
(2) Anyone who treats substances referred to in Paragraph 1 (2) or preparations, or who, by his or her activities, may affect their use by other persons, is required to treat them only to the extent strictly necessary and to avoid their use where it is possible to replace them with substances or preparations which are harmless or at least less harmful, or to influence their use in this respect.
(1) Substances and preparations to be manufactured or imported, to be treated and which can reasonably be expected to have the characteristics of poisons, narcotic substances or psychotropic substances, must be submitted with specified data and documents (Sections 4 and 26) for assessment to the Ministry of Health and Social Affairs of the Czech Socialist Republic ("the Ministry").
(2) They are required to request the assessment of substances and preparations referred to in paragraph 1,
(a) if the substances and preparations produced in the Czech Socialist Republic are the organisations which intend to introduce them into production,
(b) if the imported substances and preparations are from a domestic customer.
(3) Pending the decision on substances and preparations referred to in paragraph 1, organisations shall treat them as if they were poison or narcotic substances or psychotropic substances.
MEMBERS AND RIGHTS
Assessment of poisons
(1) The application for the assessment of a substance or preparation pursuant to Article 3 (1) shall be accompanied by:
(a) the technical standard of the substance or preparation, or, where appropriate, its proposal, or any other document containing information on its technical characteristics and main uses;
(b) particulars of the chemical composition of the substance or preparation;
(c) the results of the toxicological examination enabling the assessment of the substance or preparation, and, where appropriate, data on human experience gained from the use of the substance or preparation;
(d) the procedures by which the substance or the preparation may be disposed of or disposed of in a manner which is harmful, including procedures for the disposal of contaminated packaging, and for the disposal of the substance or preparation in solid, liquid or gaseous waste, if any.
(2) In the case of imported substances or preparations, the documents and particulars referred to in paragraph 1 (b) shall be: (b) to (d) and data on the technical characteristics of the substance or preparation shall be provided by the foreign trade undertaking or another Czechoslovak legal person or a foreign person authorised to conduct foreign commercial activity (hereinafter referred to as "the organisation authorised to do foreign business") for the domestic customer. If it is not possible to establish the exact chemical composition of the imported product, the organisation authorised for foreign trade activities shall at least indicate whether it contains the substances listed in Annex 1 or Annex 2 to this Regulation or, where appropriate, attach a declaration that the imported product does not contain those substances.
Authorisation for handling particularly hazardous poisons
(1) Only organisations authorised to do so may treat particularly dangerous poisons.
(2) At the request of the organisation, it shall issue an authorisation for the treatment of particularly hazardous poisons:
(a) the chief hygienist of the Czech Socialist Republic to an organisation which requires the import of particularly dangerous poisons, possibly an import gestor, 7)
(b) regional hygienist manufacturers,
(c) a district hygienist, unless it is reserved for a regional hygienist, in other cases.
(3) In the application for authorisation to treat particularly dangerous poisons, the organisation shall specify:
(a) the species and quantities of particularly dangerous poisons it intends to treat;
(b) the nature and manner of the intended activity;
(c) where and in what quantities particularly dangerous poisons will be stored;
(d) measures to ensure the protection of human health;
(e) measures to protect healthy living conditions, in particular ways of disposal by exhalation and waste water, disposal of solid waste or residues and contaminated packaging, and, where appropriate, measures to protect the health of foodstuffs and objects of normal use;
(f) a statement stating that persons directly managing the treatment of particularly dangerous poisons have the competence referred to in Article 15;
(g) measures to ensure particularly dangerous poisons before alienation or misuse.
(4) The authorisation shall state the name and address of the organisation, the number and date of the application, the types and quantities of particularly dangerous poisons and the types of activities covered by the authorisation, the duration of the authorisation and, where appropriate, the place of use of the particularly dangerous poisons and other particulars and conditions under which the authorisation is granted.
(5) The authorisation referred to in paragraph 2 shall also include the authorisation to re-collect particularly dangerous poisons.
(6) Disposable collection of particularly dangerous poison in the intended quantity and for the intended purpose may be authorised by the district hygienist at the request of the organisation. An organisation issuing a particularly dangerous poison shall indicate a single sample of the permit.
(7) Authorisations issued shall be kept by the authorities which issued them for a period of five years from their expiry.
(8) Universities, research and scientific institutes, as well as medical establishments, district and municipal veterinary administrations and specialised organisations of the State Veterinary Service, with the exception of organisations carrying out veterinary rendering activities (8) (hereinafter referred to as "veterinary organisations"), do not need authorisation to treat particularly dangerous poisons when they use them to perform their tasks in their establishments; However, they shall immediately communicate in writing to the county hygienist or regional hygienist, where they so reserve, the types and quantities of particularly dangerous poisons, the purpose and the manner in which they are used, including when changing the type, quantity, purpose and manner in which they are used.
Health, sale, donation and acquisition by natural persons of poisons and corrosives
(1) Particularly dangerous poisons shall not be issued, sold or donated to natural persons; natural persons shall not acquire them or otherwise.
(2) Other poisons and corrosives may not be issued, sold or donated to persons under the age of 18; such persons may not acquire them or otherwise. Other poisons and corrosives shall not be sold in food and toy stores; for self-service sales, they can only be issued by the seller.
Registration of particularly hazardous poisons
(1) The organisation is required to keep a record of the quantities produced and the quantities of particularly hazardous poisons and the reception, stock, consumption, supply and sale in the wholesale business and their disposal.
(2) The proper keeping of records of particularly dangerous poisons shall be the responsibility of the staff responsible for its management.
(3) The method of keeping records of particularly dangerous poisons is laid down in Annex 5 to this Regulation. The paper documents must be kept in such a way that the particulars contained therein cannot be amended retrospectively; the incorrect data must be corrected so that the original entry remains legible. Evidence of registration shall be kept for a period of 10 years from the end of treatment of particularly dangerous poisons.
Report on the treatment of other poisons
(1) Organisations treating other poisons are required to declare in advance their activities, the types of poisons used, their maximum annual consumption and the purpose of their use by the health service body; this obligation also applies to any change in the treatment of other poisons. Reports are not subject to other poisons used solely for chemical analysis.
(2) The reports referred to in paragraph 1 shall:
(a) organisations producing other poisons to the county hygienist; at his request, they shall indicate the name and registered office of the customer organisation;
(b) other organisations to the county hygienist or regional hygienist, if any, if they reserve it.
(3) The obligation referred to in paragraph 1 shall not apply to organisations referred to in Article 5 (8) where other poisons are used for laboratory purposes for the performance of their tasks and in their own establishments and to organisations authorised for foreign trade, where they import these substances for domestic customers.
Report on treatment of stored poison products
The organisation shall have documents containing the information necessary for the assessment of these products, in particular the type of poison used, its quantity, method and date of treatment, on the treatment of the stored food, feed and plant products and, where appropriate, on their packaging. The treatment must be reported by the organisation to the health service or, if feed is involved, to the veterinary authority. The documents shall be kept for five years from the dispatch of the treated products.
Poison and corrosive packaging
(1) Poison and corrosive substances are stored, transported and released only in packaging sufficiently solid in proportion to the weight of the contents and preventing their escape or decomposition; the weight and shape of the packed containers shall allow for safe handling and safe emptying. The closure of the packaging of particularly dangerous poisons to which it is treated must therefore be ensured that any damage is apparent.
(2) For the packaging of poisons and corrosives only packaging which is clearly different from those normally used for food and feed shall be used.
Labelling of poison and corrosive packaging
(1) The indications which must bear the packaging of the poisons and corrosives to be treated are set out in Annex 6 to this Regulation. These markings shall also be indicated in the instructions for use, prospectuses and other product documentation.
(2) The original consumer packaging (packaging for market consumption) of poisons and corrosives, with the exception of laboratory chemicals, must be accompanied by the guidelines for safe handling and instructions for the appropriate disposal of empty packaging and, where appropriate, an indication that the packaging is reversible. In addition, symptoms of poisoning and instructions for first aid must be given. This information may, where justified, be given only on the instructions for use which must be attached to each package. They must be in the Czech or Slovak language.
(3) The packaging of poisons and corrosives, where these substances or preparations are treated as laboratory chemicals, shall bear the name of the substance or preparation, the image symbol, the inscription and the weight or volume indication.
(4) In addition to the designation referred to in paragraphs 1 and 2, the chief hygienist of the Czech Socialist Republic may approve or, where justified, order the extension of the designation.
(5) The marking shall be of such size, in relation to the size of the packaging, so that it is clearly visible throughout the period of use; otherwise it shall comply with the applicable technical normal.9)
(6) The provisions of the preceding paragraphs shall not apply to consignments of imported poisons and corrosives up to the warehouse of a customer organisation designated by an organisation authorised for foreign trade, as well as to consignments of such substances or preparations in transit. However, such consignments must be marked in accordance with the relevant international transport rules.
Transport of poisons and corrosives
Specific regulations apply to the transport of poisons and corrosives. 10)
Documentation of poisons and corrosives
(1) Organisations which put into circulation substances or preparations which are poisons or corrosives are required to indicate in the documentation of these substances or preparations available to customers, sanitary services and other control authorities, in addition to the labelling and data referred to in paragraphs 1 to 4 of Article 11:
(a) the main purposes for which the substance or preparation is intended and, where appropriate, the uses thereof;
(b) the specification of the packaging of the substance or preparation in accordance with the provisions of Section 10;
(c) the procedures by which the substance or preparation can be disposed of and disposed of in a healthy manner, including procedures for the disposal of contaminated packaging, and for the disposal of the substance or preparation in solid, liquid or gaseous waste if it is also present during use.
(2) The dossier shall be submitted for approval to the chief hygienist of the Czech Socialist Republic before the substance or preparation is put into circulation, who may, on a case-by-case basis, require additional data, in particular on analytical procedures to determine the residues of the substance or preparation in crops, water and soil, while determining which of these additional data must be made available to customers, sanitary services and other control authorities pursuant to paragraph 1. Labels and instructions for use, information and promotion materials shall comply with the approved documentation.
(3) Foreign trade organisations shall cooperate with domestic customers to obtain the data referred to in the preceding paragraphs in so far as they relate to imported substances and preparations, (11) to be treated.
Notification of data on chemicals and preparations to the Toxicological Information Centre
(1) Organisations which put into circulation in the Czech Socialist Republic of chemicals or chemical products are required to notify the Toxicological Information Centre before putting them into circulation (12) the trade name, the wording of the label, the size and type of the packaging of the substance or preparation, its qualitative and quantitative composition, the purpose of the use and the method of disposal or disposal, or, if the imported substance or preparation is available, the information provided for in Section 4.
(2) The Toxicological Information Centre may, where the organisation designates them as confidential, notify only organisations which are specifically empowered by the Ministry and are bound by confidentiality. The Toxicological Information Centre shall only provide other organisations and individuals with the necessary information on first aid and treatment in cases of poisoning and other accidents with chemicals and preparations. The provisions on the protection of national, economic and professional secrets remain without prejudice. 13)
Eligibility for the treatment of poisons and corrosives
(1) Only persons who have reached 18 years of age may treat poisons and corrosives. If they are workers, they must have health and professional skills.
(2) The provisions of paragraph 1 shall not apply to persons who come into contact with poisons and corrosives during teaching or training under direct professional guidance and supervision, provided that the workplace is in such a state and work is so organised that their health and safety are not jeopardised. The persons responsible for the management and supervision of such persons shall have the necessary professional competence according to the nature of the work.
(3) Direct control of the treatment of poisons can be done by:
(a) have completed university studies in the field of medicine, veterinary medicine, pharmacy or chemistry, or in another field of study at another university, provided that he has completed his post-graduate studies in the field of industrial toxicology and as regards other health professionals, special training in which the toxicology is carried out, under specific regulations, 14); or
(b) he has completed his studies at a university other than that referred to in (a), or he has completed his studies at a secondary school through a graduate examination and successfully passed his examination before a committee for the examination of competence for poison work; or
(c) has a school education other than that referred to in (a) or (b) and has successfully passed the examination before the Commission for the examination of competence for poison work; This test shall be repeated no later than the end of the calendar year in which five years have elapsed since the previous test.
(4) Only persons having the competence referred to in paragraph 3 may sell other poisons in retail trade. The organisation shall ensure that these persons are trained once a year in the field of poisons, by the staff designated in the agreement with the regional hygienist.
(5) Workers who are active in the eradication of harmful animals, plants and micro-organisms and in the suppression of other harmful agents of poisons and do not have the capacity referred to in paragraph 3 and workers who are active in the field of protective disinfection, disinsection and extermination must take a professional course and pass the final test successfully; the test shall be repeated no later than the end of the calendar year in which three years have elapsed since the previous test. The training courses and final examinations shall be organised by the organisation and, where appropriate, by the body under its responsibility, in agreement with the county hygienist or regional hygienist.
(6) Other workers who are not referred to in paragraphs 3 to 5 and who are active in the treatment of poisons or corrosives shall be aware of the nature and effects of the substances or preparations to be treated, their handling methods, the protective measures to be followed and the principles of first aid. The organisation shall ensure that workers are familiar with this issue before work starts and that their knowledge is continuously supplemented and checked at least once a year. The organisation shall record the familiarity, complementarity and knowledge control.
(7) The medical fitness to work with poisons shall be demonstrated as a result of a preventive initial examination and periodic examination every five years, unless otherwise provided for in a specific regulation. 15)
The Commission shall examine the competence of the national committee for the work of poisons; Only an expert at a regional or district health station may be chairman. The other members shall have the expertise referred to in Article 15 (3) (a) or (b). In view of local conditions, more than one of these commissions can be established. The Commission for the examination of competence for poison work shall be of three members.
(1) The application for the test shall be submitted by the organisation whose worker is to be subjected to the test before the panel for the competence check for poison work. The application shall indicate the name and surname of the worker, the date of birth, the ID number, the education, the previous practice of working with poisons, the working grade, the work (function) to be carried out by the worker, and the names of the poisons and, where applicable, their groups with which they come into contact.
(2) The worker must demonstrate sufficient knowledge of the nature and effects of the poisons, how they are stored and transported, the hygiene and safety measures at work with them, their disposal and the principles of first aid, as well as knowledge of legislation and knowledge of the working technology of poisons. The test shall take into account the nature of the work to be done by the worker.
(3) A record of the test, a specimen of which is given in Annex 7 to this Regulation, shall be drawn up. A copy of the alert shall be sent to the organisation that submitted the application.
(4) A certificate, a specimen of which appears in Annex 8 to this Regulation, shall be issued for the test successfully carried out. The certificate shall be sent in triplicate to the organisation whose worker has passed the examination; the organisation sends one copy to the district (district) administration of the National Security Corps, and one copy to the worker.
(5) The test may be repeated no more than three times, no later than two months, and a new application shall be submitted for each test.
Operation at workplaces
The organisation shall:
(a) to ensure that the poisons or corrosives they treat do not escape into the outdoor air, soil and water, to measure their concentration as instructed by the health service authorities, and to take measures to remedy and to ensure the means for the disposal of any accident (accident) in the living and working environment caused by poisons and corrosives that are treated at the workplace;
(b) submit a proposal for a specific method of disposal or disposal of unnecessary stocks of poisons and corrosives, solid, liquid and gaseous waste containing such substances or preparations and packaging contaminated by them for approval to a district health care professional or, where appropriate, to a county hygienist;
(c) to dispose of or dispose of unnecessary stocks of the poisons and corrosives which it treats, as well as solid, liquid and gaseous wastes containing such substances or preparations and packaging contaminated by them in accordance with procedures approved by the Chief hygienist of the Czech Socialist Republic;
(d) to issue in internal operation particularly dangerous poisons from warehouses only on request, signed by a worker directly managing the treatment of particularly dangerous poisons; unprocessed or unused particularly dangerous poisons must be returned to storage or otherwise reliably secured after shift; the quantities of particularly hazardous poisons returned must be recorded.
Substances and preparations containing poisons or corrosive substances may not be put into circulation if their unnecessary stocks, solid, liquid and gaseous waste containing such substances or preparations and their contaminated packaging cannot be disposed of or disposed of in a safe and healthy manner, and even the supplier does not ensure their recovery or, where appropriate, non-safe disposal or disposal, according to current knowledge. Substances or preparations may also not be put into circulation unless the central disposal or disposal of their waste is ensured by a regional hygienist or a major hygienist of the Czech Socialist Republic.
The organisation shall ensure that unauthorised persons do not have access to poisons; the loss or theft of the poison shall be notified without delay to the nearest department of the National Security Corps.
(1) Organisations are required to issue rules for workplaces where poisons and corrosives are handled, or for individual types of work (technology), 16) in which the necessary safety and protective measures, including emergency measures, must be laid down under specific conditions. These rules are approved by a district hygienist or regional hygienist or chief hygienist of the Czech Socialist Republic in cases where they reserve it.
(2) The rules must include in particular:
(a) safe handling and disposal of poisons and corrosives, including packaging after use;
(b) a list of the means and equipment available for human protection, effective disposal of these substances as well as for the protection of healthy living conditions and guidelines for first aid when dealing with poisons and corrosives;
(c) the manner in which poisons and corrosives may be stored with other substances, in particular in view of the possibility of developing substances which are even more dangerous or of other accidents.
(3) Organisations shall be required to provide evidence of the rules of all persons involved in the treatment of poisons and corrosives and to verify at least once a year the knowledge of those rules. The rules must be posted at workplaces in a visible and accessible place.
Storage of poisons
(1) The room in which poisons are stored must be locked, protected against burglary and cannot contain narcotic substances, psychotropic substances, medicines, food, feed or explosives.
(2) Particularly dangerous poisons may be stored in one room with substances or preparations other than those referred to in paragraph 1 only if they are stored in a locked box intended solely for the storage of poisons. With other poisons, particularly dangerous poisons may be stored in one room or in one box, if they are stored separately and their harmful effects or confusion are excluded, and such storage arrangements have been approved by the health service authority.
(3) Other poisons may be stored together with substances or preparations which are not poisons, with the exception of those referred to in paragraph 1, in one room or, where appropriate, in one container, if they are stored separately and their harmful effects or confusion are excluded.
(4) Poison placed in tanks or in similar large containers or packaging may be stored in enclosed spaces secured against adverse climatic conditions, against harmful effects of poisons on the surrounding area and against unauthorised entry into those areas.
Professional supervision
The health care services shall be carried out by the health authorities when dealing with poisons and corrosives. 17) In carrying out their tasks, they shall also be entitled to check the established records of particularly dangerous poisons.
Specific authorisation
The health services authorities shall be entitled to:
(a) withdraw authorisations granted pursuant to Article 5 of this Regulation if the conditions laid down or determined are not complied with;
(b) prohibit the use of poisons and corrosives or products treated by them for certain purposes and, where appropriate, provide that they may be used only for certain purposes specifically defined or only under certain conditions;
(c) prohibit the use of poisons and corrosive substances by organisations and natural persons, or prohibit their use at certain workplaces, if significant defects are detected in checking;
(d) order the proficiency check of persons referred to in § 15 (3) to (6) of the Commission for the proficiency check for poison work;
(e) prohibit workers from working with poisons and corrosives or from managing such work if they find that such persons, out of ignorance, insubordination or because of their health, endanger the health and lives of other people or their own health or life at work;
(f) lay down specific measures for the security and disposal of waste containing poisons.
Emission of harmful animals, plants and micro-organisms and suppression of other harmful agents of poisons
(1) The use of poisons for the control of harmful animals, plants and micro-organisms and the suppression of other harmful agents in closed premises shall be notified to the health service body at least 48 hours before the start of the action, except for measures to control outbreaks of dangerous and very dangerous animal diseases, 18) when it is sufficient to make a notification before the start of the action. The organisation's notification shall specify:
(a) the precise designation of the object where the destruction will be carried out;
(b) the area (cubatura) of the object or room, and, if it comes to warehouses, the type of goods stored,
(c) the type, approximate quantity and concentration of poisons to be used; the use of particularly hazardous gaseous poisons (e.g. hydrogen cyanide) must be specifically marked;
(d) the necessary preparatory work and the time needed for its implementation;
(e) the day and hour of the start of the event,
(f) the duration of the operation and the time needed to implement the action;
(g) the security measures to be implemented;
(h) the name and address of the implementing organisation and the name and address of the official responsible.
(2) The use of poisons for the control of harmful animals, plants and micro-organisms and the suppression of other harmful agents at sites other than those referred to in paragraph 1 shall be notified by the organisation to the health service authority and to the local (urban) national committee within whose perimeter these poisons will be used at least 48 hours before the start of the action, except in cases of sudden infestation of the crops by dangerous pests and diseases where it is sufficient to make a notification before the start of the action. The organisation shall notify the action in writing of the air application. The organisation's notification shall specify:
(a) precise identification of the place where the action will be carried out and how it will be implemented;
(b) the type, approximate quantity and concentration of poisons to be used;
(c) the pest against which the poison will be used;
(d) the day and hour of the start of the action;
(e) the expected duration of the action;
(f) the security measures to be implemented;
(g) the name and address of the implementing organisation and the name and address of the official responsible.
(3) The use of poisons for the control of harmful animals, plants and micro-organisms and the suppression of other harmful agents in closed premises or other places intended for animals, food, raw materials of animal origin or feed shall also be notified to the veterinary authority. 19)
(4) The working days shall not be counted within the 48-hour period referred to in paragraphs 1 and 2. Actions may be initiated only if the health service or veterinary administration has not otherwise provided for at least 24 hours before the start of the action. In addition, health services and veterinary administration may lay down specific conditions for work.
(5) The actions referred to in paragraphs 1 and 2 may be carried out only in accordance with the working procedures and, where appropriate, with the technical rules approved by the health service authority. 17)
OMINOUS SUBSTANCES AND PSYCHOTROPIC SUBSTANCES
Assessment of narcotic substances and psychotropic substances
The application for the assessment of a narcotic substance, psychotropic substance or preparation referred to in Article 3 (1) shall be supported by a method laid down by specific provisions. 20)
Authorisation for the treatment of narcotic substances and psychotropic substances
(1) Only organisations authorised to do so may treat narcotic substances and psychotropic substances or preparations, unless otherwise specified.
(2) Narcotic substances, with the exception of those listed in Group III, and psychotropic substances, with the exception of those listed in Group I, may be handled without authorisation only by medical establishments, veterinary organisations, health science, educational, research and control institutes and workplaces, supply organisations, if they are required to perform their tasks.
(3) Authorisations for the treatment of narcotic substances and psychotropic substances or preparations are issued by the Ministry at the request of the organisation.
(4) In the application for authorisation to handle narcotic substances and psychotropic substances or preparations, the organisation shall indicate:
(a) the precise labelling of the narcotic drugs and psychotropic substances or preparations they intend to treat;
(b) the nature and extent of the intended activity;
(c) measures against the misuse of narcotic drugs and psychotropic substances or preparations and against harm to human health;
(d) a statement stating that the persons responsible for the treatment and registration of narcotic substances and psychotropic substances or preparations have the competence referred to in Article 34.
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Regulation Information
| Citation | Decree of the Government of the Czech Socialist Republic No. 192 / 1988 Coll., on poisons and certain other harmful health substances |
|---|---|
| Regulation Type | - |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 14.12.1988 |
|---|---|
| Effective from | 01.01.1989 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
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